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1 Ergebnisse
1
Genome-wide association analyses identify new risk variants..:
Van Rheenen, Wouter
;
Shatunov, Aleksey
;
Dekker, Annelot M
...
info:eu-repo/semantics/altIdentifier/pmid/27455348. , 2016
Link:
http://hdl.handle.net/11586/214286
RT Journal T1
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
UL https://suche.suub.uni-bremen.de/peid=base-ftunivbari:oai:ricerca.uniba.it:11586_214286&Exemplar=1&LAN=DE A1 Van Rheenen, Wouter A1 Shatunov, Aleksey A1 Dekker, Annelot M A1 McLaughlin, Russell L A1 Diekstra, Frank P A1 Pulit, Sara L A1 Van Der Spek, Rick A. A A1 Võsa, Urmo A1 De Jong, Simone A1 Robinson, Matthew R A1 Yang, Jian A1 Fogh, Isabella A1 Van Doormaal, Perry T. C A1 Tazelaar, Gijs H. P A1 Koppers, Max A1 Blokhuis, Anna M A1 Sproviero, William A1 Jones, Ashley R A1 Kenna, Kevin P A1 Van Eijk, Kristel R A1 Harschnitz, Oliver A1 Schellevis, Raymond D A1 Brands, William J A1 Medic, Jelena A1 Menelaou, Androniki A1 Vajda, Alice A1 Ticozzi, Nicola A1 Lin, Kuang A1 Rogelj, Boris A1 Vrabec, Katarina A1 Ravnik-Glava, Metka A1 Koritnik, Bla A1 Zidar, Janez A1 Leonardis, Lea A1 Grošelj, Leja Dolenc A1 Millecamps, Stéphanie A1 Salachas, François A1 Meininger, Vincent A1 De Carvalho, Mamede A1 Pinto, Susana A1 Mora, Jesus S A1 Rojas-García, Ricardo A1 Polak, Meraida A1 Chandran, Siddharthan A1 Colville, Shuna A1 Swingler, Robert A1 Morrison, Karen E A1 Shaw, Pamela J A1 Hardy, John A1 Orrell, Richard W A1 Pittman, Alan A1 Sidle, Katie A1 Fratta, Pietro A1 Malaspina, Andrea A1 Topp, Simon A1 Petri, Susanne A1 Abdulla, Susanne A1 Drepper, Carsten A1 Sendtner, Michael A1 Meyer, Thomas A1 Ophoff, Roel A A1 Staats, Kim A A1 Wiedau-Pazos, Martina A1 Lomen-Hoerth, Catherine A1 Van Deerlin, Vivianna M A1 Trojanowski, John Q A1 Elman, Lauren A1 McCluskey, Leo A1 Basak, A Nazli A1 Tunca, Ceren A1 Hamzeiy, Hamid A1 Parman, Yesim A1 Meitinger, Thomas A1 Lichtner, Peter A1 Radivojkov-Blagojevic, Milena A1 Andres, Christian R A1 Maurel, Cindy A1 Bensimon, Gilbert A1 Landwehrmeyer, Bernhard A1 Brice, Alexis A1 Payan, Christine A. M A1 Saker-Delye, Safaa A1 Dürr, Alexandra A1 Wood, Nicholas W A1 Tittmann, Lukas A1 Lieb, Wolfgang A1 Franke, Andre A1 Rietschel, Marcella A1 Cichon, Sven A1 Nöthen, Markus M A1 Amouyel, Philippe A1 Tzourio, Christophe A1 Dartigues, Jean-François A1 Uitterlinden, Andre G A1 Rivadeneira, Fernando A1 Estrada, Karol A1 Hofman, Albert A1 Curtis, Charles A1 Blauw, Hylke M A1 Van Der Kooi, Anneke J A1 De Visser, Marianne A1 Goris, An A1 Weber, Markus A1 Shaw, Christopher E A1 Smith, Bradley N A1 Pansarasa, Orietta A1 Cereda, Cristina A1 Del Bo, Roberto A1 Comi, Giacomo P A1 D'Alfonso, Sandra A1 Bertolin, Cinzia A1 Sorarù, Gianni A1 Mazzini, Letizia A1 Pensato, Viviana A1 Gellera, Cinzia A1 Tiloca, Cinzia A1 Ratti, Antonia A1 Calvo, Andrea A1 Moglia, Cristina A1 Brunetti, Maura A1 Arcuti, Simona A1 Capozzo, Rosa A1 Zecca, Chiara A1 Lunetta, Christian A1 Penco, Silvana A1 Riva, Nilo A1 Padovani, Alessandro A1 Filosto, Massimiliano A1 Muller, Bernard A1 Stuit, Robbert Jan A1 Blair, Ian A1 Zhang, Katharine A1 McCann, Emily P A1 Fifita, Jennifer A A1 Nicholson, Garth A A1 Rowe, Dominic B A1 Pamphlett, Roger A1 Kiernan, Matthew C A1 Grosskreutz, Julian A1 Witte, Otto W A1 Ringer, Thomas A1 Prell, Tino A1 Stubendorff, Beatrice A1 Kurth, Ingo A1 Hübner, Christian A A1 Nigel Leigh, P A1 Casale, Federico A1 Chio, Adriano A1 Beghi, Ettore A1 Pupillo, Elisabetta A1 Tortelli, Rosanna A1 Logroscino, Giancarlo A1 Powell, John A1 Ludolph, Albert C A1 Weishaupt, Jochen H A1 Robberecht, Wim A1 Van Damme, Philip A1 Franke, Lude A1 Pers, Tune H A1 Brown, Robert H A1 Glass, Jonathan D A1 Landers, John E A1 Hardiman, Orla A1 Andersen, Peter M A1 Corcia, Philippe A1 Vourc'H, Patrick A1 Silani, Vincenzo A1 Wray, Naomi R A1 Visscher, Peter M A1 De Bakker, Paul I. W A1 Van Es, Michael A A1 Jeroen Pasterkamp, R A1 Lewis, Cathryn M A1 Breen, Gerome A1 Al-Chalabi, Ammar A1 Van Den Berg, Leonard H A1 Veldink, Jan H YR 2016 K1 Amyotrophic Lateral Sclerosi K1 Case-Control Studie K1 Cohort Studie K1 Genome-Wide Association Study K1 Human K1 Munc18 Protein K1 Mutation K1 Myelin Protein K1 Netherland K1 Protein K1 Genetic Predisposition to Disease K1 Genetics JF info:eu-repo/semantics/altIdentifier/pmid/27455348 LK http://hdl.handle.net/11586/214286 DO http://hdl.handle.net/11586/214286 SF ELIB - SuUB Bremen
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